Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388307Generated: October 29, 2026

Ethyl (2R)-2-methyl-5-(propan-2-ylidene)cyclopentane-1-carboxylate → Ethyl (2R)-2-methyl-5-oxocyclopentane-1-carboxylate

https://huagongshe.com/reaction/388307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (2R)-2-methyl-5-(propan-2-ylidene)cyclopentane-1-carboxylateHCID 11830361—
ReactantIsopropanol carbon dioxideHCID 86586944—
SolventEthyl AcetateHCID 8857—
ProductEthyl (2R)-2-methyl-5-oxocyclopentane-1-carboxylateHCID 1105207596%

Reaction Steps

(2R)-Ethyl 2-methyl-5-(propan-2-ylidene)cyclopentanecarboxylate (24 g, 0.122 mol) in ethyl acetate (100 mL) was cooled to −68° C. with dry ice/isopropanol. Ozonized oxygen (5-7 ft3h−1 of O2) was bubbled through the solution for 3.5 hours. The reaction mixture was flushed with nitrogen at room temperature until the color disappeared. The ethyl acetate was removed under vacuum, and the residue was dissolved in acetic acid (150 mL) and cooled by ice water. Zinc powder (45 g) was then added. The solution was stirred for 30 minutes and then filtered. The filtrate was neutralized with 2N NaOH (1.3 L) and NaHCO3. The aqueous phase was extracted with ether (3×200 mL). The organic phase was combined, washed with water, dried and concentrated to afford (2R)-ethyl 2-methyl-5-oxocyclopentanecarboxylate (20 g, 96%). 1H NMR (CDCl3, 400 MHz) δ 4.21 (m, 2H), 2.77 (d, J=11.2 Hz, 1H), 2.60 (m, 1H), 2.50-2.10 (m, 3H), 1.42 (m, 1H), 1.33 (m, 3H), 1.23 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377937B2
Source datasetuspto-grants-2013_02
ORD IDord-1ca75867a8db46c292230a55758a3d9b
Source noteuspto-grants-2013_02